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Resequencing of Pooled DNA for Detecting Disease Associations with Rare Variants
A combination of common and rare variants is thought to contribute to genetic susceptibility to complex diseases. Recently, next-generation sequencers have greatly lowered sequencing costs, providing an opportunity to identify rare disease variants in large genetic epidemiology studies. At present,...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2010
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4096227/ https://ncbi.nlm.nih.gov/pubmed/20578089 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.20502 |
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